Methyl 3,6,8-trihydroxy-4-methoxy-1-methyl-9,10-dioxoanthracene-2-carboxylate

Details

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Internal ID 780df50c-6890-4f61-a0cb-3da2392dc1f0
Taxonomy Benzenoids > Anthracenes > Anthracenecarboxylic acids and derivatives > Anthracenecarboxylic acids
IUPAC Name methyl 3,6,8-trihydroxy-4-methoxy-1-methyl-9,10-dioxoanthracene-2-carboxylate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C18H14O8/c1-6-10-13(17(25-2)16(23)11(6)18(24)26-3)14(21)8-4-7(19)5-9(20)12(8)15(10)22/h4-5,19-20,23H,1-3H3
InChI Key QQKYEIPWELLTRP-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C18H14O8
Molecular Weight 358.30 g/mol
Exact Mass 358.06886740 g/mol
Topological Polar Surface Area (TPSA) 130.00 Ų
XlogP 3.10
Atomic LogP (AlogP) 1.68
H-Bond Acceptor 8
H-Bond Donor 3
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Methyl 3,6,8-trihydroxy-4-methoxy-1-methyl-9,10-dioxoanthracene-2-carboxylate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9523 95.23%
Caco-2 + 0.5750 57.50%
Blood Brain Barrier - 0.8000 80.00%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Mitochondria 0.6709 67.09%
OATP2B1 inhibitior - 0.7051 70.51%
OATP1B1 inhibitior + 0.8764 87.64%
OATP1B3 inhibitior - 0.4389 43.89%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.6821 68.21%
P-glycoprotein inhibitior - 0.7205 72.05%
P-glycoprotein substrate - 0.8495 84.95%
CYP3A4 substrate + 0.5659 56.59%
CYP2C9 substrate - 0.8134 81.34%
CYP2D6 substrate - 0.8475 84.75%
CYP3A4 inhibition - 0.8673 86.73%
CYP2C9 inhibition - 0.8537 85.37%
CYP2C19 inhibition - 0.9630 96.30%
CYP2D6 inhibition - 0.8931 89.31%
CYP1A2 inhibition - 0.5627 56.27%
CYP2C8 inhibition + 0.6182 61.82%
CYP inhibitory promiscuity - 0.7915 79.15%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9075 90.75%
Carcinogenicity (trinary) Non-required 0.6066 60.66%
Eye corrosion - 0.9890 98.90%
Eye irritation + 0.6091 60.91%
Skin irritation - 0.7152 71.52%
Skin corrosion - 0.9508 95.08%
Ames mutagenesis + 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7694 76.94%
Micronuclear + 0.8100 81.00%
Hepatotoxicity + 0.6875 68.75%
skin sensitisation - 0.9191 91.91%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity + 0.6222 62.22%
Mitochondrial toxicity + 0.6000 60.00%
Nephrotoxicity + 0.6019 60.19%
Acute Oral Toxicity (c) II 0.5957 59.57%
Estrogen receptor binding + 0.8186 81.86%
Androgen receptor binding - 0.5418 54.18%
Thyroid receptor binding - 0.5455 54.55%
Glucocorticoid receptor binding + 0.6469 64.69%
Aromatase binding - 0.5662 56.62%
PPAR gamma + 0.5791 57.91%
Honey bee toxicity - 0.9164 91.64%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.5900 59.00%
Fish aquatic toxicity + 0.9844 98.44%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.71% 91.11%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 95.18% 99.23%
CHEMBL2581 P07339 Cathepsin D 94.08% 98.95%
CHEMBL1951 P21397 Monoamine oxidase A 91.29% 91.49%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 90.84% 99.15%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.15% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.75% 89.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.47% 94.00%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 88.47% 96.38%
CHEMBL4208 P20618 Proteasome component C5 87.64% 90.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.61% 96.09%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 86.49% 94.42%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 84.95% 91.07%
CHEMBL2535 P11166 Glucose transporter 83.95% 98.75%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.04% 99.17%
CHEMBL3401 O75469 Pregnane X receptor 82.28% 94.73%
CHEMBL340 P08684 Cytochrome P450 3A4 82.15% 91.19%
CHEMBL2056 P21728 Dopamine D1 receptor 81.16% 91.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.51% 86.33%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Eleutherine bulbosa

Cross-Links

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PubChem 46201084
LOTUS LTS0216898
wikiData Q105225909